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The mature mesonephric nephron of the rabbit embryo

III. Freeze-fracture studies

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Summary

In freeze-fracture replicas of the entire cross-fractured mesonephros of 18 day rabbit embryos the basolateral and luminal cell faces of the different nephron segments were studied and compared with their metanephric counterparts. In the proximal tubule, the shallow zonula occludens exhibited only 1–2 strands and resembled the corresponding metanephric zonula, a very “leaky” type, which was found with a considerable paracellular flow component in sites of isotonic reabsorption. Gap junctions were restricted to the proximal tubule and were seen more frequently in its terminal segment. The distal tubule harboured two types of tight junctions. The most common type, a band of 5–8 closely parallel strands, matched the zonula occludens of the metanephric straight distal tubule. The observed particle density of the basolateral membrane (2,500±328/μm2) was less than that of the proximal tubule (2,642±306). In addition, the collecting tubule exhibited a zonula occludens of the “tight” variety similar to that which occurred in the metanephric collecting duct. Rod-shaped particles of the luminal membrane were mainly concentrated in some of the intercalated cells but also had developed on principal cells, and occasionally, in the distal tubule. The Wolffian duct, with a deep “tight” zonula occludens, had an obviously rather inactive epithelium with no conspicuous transport-linked membrane specializations.

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References

  • Bindslev N, Tormey J McD, Wright EM (1974) The effects of electrical and osmotic gradients on lateral intercellular spaces and membrane conductance in a low resistance epithelium. J Mebr Biol 19:357–380

    Google Scholar 

  • Burg MG, Green N (1973) Function of the thick ascending limb of Henle's loop. Am J Physiol 244:659–668

    Google Scholar 

  • Claude Ph (1978) Morphological factors influencing transepithelial permeability: A model for the resistance of the zonula occludens. J Membr Biol 39:219–232

    Google Scholar 

  • Claude Ph, Goodenough DA (1973) Fracture faces of zonulae occludentes from “tight” and “leaky” epithelia. J Cell Biol 58:390–400

    Google Scholar 

  • Davies J, Routh JI (1957) Composition of the foetal fluids of the rabbit. J Embryol Exp Morphol 5:32–39

    Google Scholar 

  • Di Bona DR, Mills JW (1979) Distribution of Na+-pump sites in transporting epithelia. Fed Proc 38:134–143

    Google Scholar 

  • Ernst SA, Dodsen WC, Karnaky KJ (1980) Structural diversity of occluding junctions in the lowresistance chloride-secreting opercular epithelium of seawater-adapted killifish (Fundulus hetero- clitus). J Cell Biol 87:488–497

    Google Scholar 

  • Farquhar MG, Palade GE (1963) Junctional complexes in various epithelia. J Cell Biol 17:375–412

    Google Scholar 

  • Frederiksen O, Møllgard K, Rostgaard J (1979) Lack of correlation between transepithelial transport capacity and paracellular pathway ultrastructure in alcian blue-treated rabbit gallbladders. J Cell Biol 83:383–393

    Google Scholar 

  • Frömter E (1972) The route of passive ion movement through the epithelium of Necturus gallbladder. J Membr Biol 8:259–301

    Google Scholar 

  • Humbert F, Pricam C, Perrelet A, Orci L (1975) Specific plasma membrane differentiations in the cells of the kidney collecting tubule. J Ultrastr Res 52:13–20

    Google Scholar 

  • Humbert F, Grandchamp A, Pricam C, Perrelet A, Orci L (1976) Morphological changes in tight junctions of Necturus maculosus proximal tubules undergoing saline diuresis. J Cell Biol 69:90–96

    Google Scholar 

  • Huss RE, Marsh DJ (1975) A model of NaCl and water flow through paracellular pathways of renal proximal tubules. J Membr Biol 23:305–347

    Google Scholar 

  • Kaissling B, Kriz W (1979) Structural analysis of the rabbit kidney. Adv Anat Embryol 56:1–121

    Google Scholar 

  • Kriz W, Schiller A, Kaissling B, Taugner R (1980) Comparative and functional aspects of the thin limb ultrastructure. In: Maunsbach AB, Ølsen TS, Christensen EI (eds) Functional ultrastructure of the kidney. Academic Press, London 17:239–250

    Google Scholar 

  • Kriz W, Schiller A, Taugner R (1981) Freeze-fracture studies on the thin limbs of Henle's loop in Psammomys obesus. Am J Anat (in press)

  • Kühn K, Reale E (1975) Junctional complexes of the tubular cells in the human kidney as revealed with freeze-fracture. Cell Tissue Res 160:193–205

    Google Scholar 

  • Lewis FT (1920) The course of the Wolffian tubules in mammalian embryos. Am J Anat 26:423–435

    Google Scholar 

  • Machen TE, Erlij D, Wooding FBP (1972) Permeable Junctional complexes. J Cell Biol 54:302–312

    Google Scholar 

  • Malnic G, Giebisch G (1972) Some electrical properties of distal tubular epithelium in the rat. Am J Physiol 223:797–808

    Google Scholar 

  • Martínez-Palomo A, Erlij D (1975) Structure of tight junctions in epithelia with different permeability. Proc Natl Acad Sci USA 72:4487–4491

    Google Scholar 

  • Martínez-Palomo A, Meza I, Beaty G, Cereijido M (1980) Experimental modulation of occluding junctions in a cultured transporting epithelium. J Cell Biol 87:736–745

    Google Scholar 

  • Meldolesi J, Castiglione G, Parma R, Nassivera N, De Camilli P (1978) Ca++ dependent disassembly and reassembly of occluding junctions in guinea pig pancreatic acinar cells. Effect of drugs. J Cell Biol 79:156–172

    Google Scholar 

  • Meza I, Iberra G, Sabanero M, Martínez-Paloma A, Cereijido M (1980) Occluding junctions and cytoskeletal components in a cultured transporting epthelium. J Cell Biol 87:746–754

    Google Scholar 

  • Minuth M (1980) Die Differenzierung der Zell-Zellverbindungen und die Entstehung des juxtaglomerulären Apparates in der reifenden Säugerniere: Diss. Köln

  • Oschmann JL (1978) Morphological correlates of transport. In: Giebisch G, Tosteson DC, Ussing HH (eds) Membrane transport in biology. Springer Verlag, Berlin Heidelberg New York, Vol III, chapt 3, pp 67–93

    Google Scholar 

  • Peek W, Shivers RR, McMillan DB (1977) Freeze-fracture analysis of Junctional complexes in the nephron of the garter snake, Thamnophis sirtalis. Cell Tissue Res 179:441–451

    Google Scholar 

  • Pricam C, Humbert F, Perrelet A, Orci L (1974) A freeze-etch study of the tight junctions of the rat kidney tubules. Lab Invest 30:286–291

    Google Scholar 

  • Riddle CV, Ernst SA (1979) Structural simplicity of the zonula occludens in the electrolyte secreting epithelium of the avian salt gland. J Membr Biol 45:21–35

    Google Scholar 

  • Roesinger B, Schiller A, Taugner L (1978) A freeze-fracture study of tight junctions in the pars convoluta and pars recta of the renal proximal tubule. Cell Tissue Res 186:121–133

    Google Scholar 

  • Sackin H, Boulpaep EL (1975) Models for coupling of salt and water transport. Proximal tubular reabsorption in Necturus kidney. J Gen Physiol 66:671–733

    Google Scholar 

  • Schiller A, Taugner R, Kriz W (1980a) The thin limbs of Henle's loop in the rabbit. A freeze fracture study. Cell Tissue Res 207:249–265

    Google Scholar 

  • Schiller A, Forssmann WG, Taugner R (1980b) The tight junctions of the renal tubules in the cortex and outer medulla. A quantitative study of the kidneys of six species. Cell Tissue Res 212:395–413

    Google Scholar 

  • Stetson DL, Wade JB, Giebisch G (1980) Morphologic alterations in the rat medullary collecting duct following potassium depletion. Kidney Int 17:45–56

    Google Scholar 

  • Suzuki F, Nagano T (1978) Development of tight junctions in the caput epididymal epithelium of the mouse. Dev Biol 63:321–334

    Google Scholar 

  • Taugner R, Boll U, Zahn P, Forssmann WG (1976) Cell junctions in the epithelium of Bowman's capsule. Cell Tissue Res 172:431–446

    Google Scholar 

  • Tiedemann K (1979) Architecture of the mesonephric nephron in pig and rabbit. Anat Embryol 157:105–112

    Google Scholar 

  • Tiedemann K, Wettstein R (1980) The mature mesonephric nephron of the rabbit embroy. I. SEM-studies. Cell Tissue Res 209:95–109

    Google Scholar 

  • Ullrich KJ, Frömter E, Murer H (1979) Prinzipien des epithelialen Transportes in Niere und Darm. Klin Wochenschr 57:977–991

    Google Scholar 

  • nVan Deurs B, Koehler JK (1979) Tight junctions in the choroid plexus epithelium. J Cell Biol 80:662–673

    Google Scholar 

  • Wettstein R, Tiedemann K (1981) The mature mesonephric nephron of the rabbit embryo. II. TEM-studies. Cell Tissue Res 218:161–180

    Google Scholar 

  • Wright EM, Diamond JM (1968) Effects of pH and polyvalent cations on the selective permeability of gallbladder epithelium to monovalent ions. Biochim Biophys Acta 163:57–74

    Google Scholar 

  • Wright FS (1971) Increasing magnitude of electrical potential along the renal distal tubule. Am J Physiol 220:624–638

    Google Scholar 

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Schiller, A., Tiedemann, K. The mature mesonephric nephron of the rabbit embryo. Cell Tissue Res. 221, 431–442 (1981). https://doi.org/10.1007/BF00216746

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